Canonical Allele Identifier: PA198969
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 188618
ClinVar RCV Id: RCV000810318 RCV001180801 RCV003317124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala938Ser
CA013131
NM_000257.4:c.2812G>T